Assessing User Satisfaction and Adherence to an Abbreviated Dietary Tracking App (MySnackTracker) Versus Full-intake Dietary Monitoring

Part of paid clinical trials in Houston, Texas.

Sponsor
M.D. Anderson Cancer Center
Study ID
NCT06919471
Status
Recruiting

Conditions

  • Dietary Monitoring

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Fitbit — OTHER
    Wear it on wrist
  • MySnackTracker App — OTHER
    App to track your dietary intake

Study Details

To learn if a method of abbreviated food tracking (called MySnackTracker) is a reasonable alternative to traditional full-intake food tracking and to compare the adherence to and acceptability of each method.

Key Dates

Start date
Apr 8, 2025
Status verified
May 2026
Primary completion
May 1, 2028
Completion
May 1, 2030

Study Design

Enrollment
90 participants (estimated)
Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH

Arms

  • Experimental: Group 2: Fitbit
    Participants in Group 2, will use the Fitbit food logging app to track their dietary intake. Participants will be asked to log all food and drink intake.
  • Experimental: Group 1: MySnackTracker
    Participants in Group 1 will use MySnackTracker to track their dietary intake. Participants will be asked to log only high-calorie, low-nutrient food and drinks, or snacks" (for example, cookies, chips and dip, and alcohol). A full list of these foods and drinks is provided in the app.

Primary Outcome Measure

Safety and adverse events [ Time Frame: Through study completion; an average of 1 year ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
MD Anderson Cancer CenterHoustonTexas77030
Karen M Basen-Engquist, MD
Karen M Basen-Engquist, MD (PRINCIPAL_INVESTIGATOR)

Find similar trials in Houston, TX